CN104004351A - High-glass-fiber reinforced nylon material and preparing method of high-glass-fiber reinforced nylon material - Google Patents
High-glass-fiber reinforced nylon material and preparing method of high-glass-fiber reinforced nylon material Download PDFInfo
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- CN104004351A CN104004351A CN201410017562.7A CN201410017562A CN104004351A CN 104004351 A CN104004351 A CN 104004351A CN 201410017562 A CN201410017562 A CN 201410017562A CN 104004351 A CN104004351 A CN 104004351A
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- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
- C08L77/00—Compositions of polyamides obtained by reactions forming a carboxylic amide link in the main chain; Compositions of derivatives of such polymers
- C08L77/06—Polyamides derived from polyamines and polycarboxylic acids
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- B—PERFORMING OPERATIONS; TRANSPORTING
- B29—WORKING OF PLASTICS; WORKING OF SUBSTANCES IN A PLASTIC STATE IN GENERAL
- B29B—PREPARATION OR PRETREATMENT OF THE MATERIAL TO BE SHAPED; MAKING GRANULES OR PREFORMS; RECOVERY OF PLASTICS OR OTHER CONSTITUENTS OF WASTE MATERIAL CONTAINING PLASTICS
- B29B9/00—Making granules
- B29B9/12—Making granules characterised by structure or composition
- B29B9/14—Making granules characterised by structure or composition fibre-reinforced
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- B—PERFORMING OPERATIONS; TRANSPORTING
- B29—WORKING OF PLASTICS; WORKING OF SUBSTANCES IN A PLASTIC STATE IN GENERAL
- B29B—PREPARATION OR PRETREATMENT OF THE MATERIAL TO BE SHAPED; MAKING GRANULES OR PREFORMS; RECOVERY OF PLASTICS OR OTHER CONSTITUENTS OF WASTE MATERIAL CONTAINING PLASTICS
- B29B7/00—Mixing; Kneading
- B29B7/30—Mixing; Kneading continuous, with mechanical mixing or kneading devices
- B29B7/58—Component parts, details or accessories; Auxiliary operations
- B29B7/72—Measuring, controlling or regulating
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- B—PERFORMING OPERATIONS; TRANSPORTING
- B29—WORKING OF PLASTICS; WORKING OF SUBSTANCES IN A PLASTIC STATE IN GENERAL
- B29B—PREPARATION OR PRETREATMENT OF THE MATERIAL TO BE SHAPED; MAKING GRANULES OR PREFORMS; RECOVERY OF PLASTICS OR OTHER CONSTITUENTS OF WASTE MATERIAL CONTAINING PLASTICS
- B29B7/00—Mixing; Kneading
- B29B7/74—Mixing; Kneading using other mixers or combinations of mixers, e.g. of dissimilar mixers ; Plant
- B29B7/7461—Combinations of dissimilar mixers
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- B—PERFORMING OPERATIONS; TRANSPORTING
- B29—WORKING OF PLASTICS; WORKING OF SUBSTANCES IN A PLASTIC STATE IN GENERAL
- B29B—PREPARATION OR PRETREATMENT OF THE MATERIAL TO BE SHAPED; MAKING GRANULES OR PREFORMS; RECOVERY OF PLASTICS OR OTHER CONSTITUENTS OF WASTE MATERIAL CONTAINING PLASTICS
- B29B7/00—Mixing; Kneading
- B29B7/80—Component parts, details or accessories; Auxiliary operations
- B29B7/88—Adding charges, i.e. additives
- B29B7/90—Fillers or reinforcements, e.g. fibres
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- B—PERFORMING OPERATIONS; TRANSPORTING
- B29—WORKING OF PLASTICS; WORKING OF SUBSTANCES IN A PLASTIC STATE IN GENERAL
- B29B—PREPARATION OR PRETREATMENT OF THE MATERIAL TO BE SHAPED; MAKING GRANULES OR PREFORMS; RECOVERY OF PLASTICS OR OTHER CONSTITUENTS OF WASTE MATERIAL CONTAINING PLASTICS
- B29B9/00—Making granules
- B29B9/12—Making granules characterised by structure or composition
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B29—WORKING OF PLASTICS; WORKING OF SUBSTANCES IN A PLASTIC STATE IN GENERAL
- B29C—SHAPING OR JOINING OF PLASTICS; SHAPING OF MATERIAL IN A PLASTIC STATE, NOT OTHERWISE PROVIDED FOR; AFTER-TREATMENT OF THE SHAPED PRODUCTS, e.g. REPAIRING
- B29C48/00—Extrusion moulding, i.e. expressing the moulding material through a die or nozzle which imparts the desired form; Apparatus therefor
- B29C48/25—Component parts, details or accessories; Auxiliary operations
- B29C48/36—Means for plasticising or homogenising the moulding material or forcing it through the nozzle or die
- B29C48/395—Means for plasticising or homogenising the moulding material or forcing it through the nozzle or die using screws surrounded by a cooperating barrel, e.g. single screw extruders
- B29C48/40—Means for plasticising or homogenising the moulding material or forcing it through the nozzle or die using screws surrounded by a cooperating barrel, e.g. single screw extruders using two or more parallel screws or at least two parallel non-intermeshing screws, e.g. twin screw extruders
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- B—PERFORMING OPERATIONS; TRANSPORTING
- B29—WORKING OF PLASTICS; WORKING OF SUBSTANCES IN A PLASTIC STATE IN GENERAL
- B29C—SHAPING OR JOINING OF PLASTICS; SHAPING OF MATERIAL IN A PLASTIC STATE, NOT OTHERWISE PROVIDED FOR; AFTER-TREATMENT OF THE SHAPED PRODUCTS, e.g. REPAIRING
- B29C48/00—Extrusion moulding, i.e. expressing the moulding material through a die or nozzle which imparts the desired form; Apparatus therefor
- B29C48/25—Component parts, details or accessories; Auxiliary operations
- B29C48/92—Measuring, controlling or regulating
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B29—WORKING OF PLASTICS; WORKING OF SUBSTANCES IN A PLASTIC STATE IN GENERAL
- B29B—PREPARATION OR PRETREATMENT OF THE MATERIAL TO BE SHAPED; MAKING GRANULES OR PREFORMS; RECOVERY OF PLASTICS OR OTHER CONSTITUENTS OF WASTE MATERIAL CONTAINING PLASTICS
- B29B7/00—Mixing; Kneading
- B29B7/30—Mixing; Kneading continuous, with mechanical mixing or kneading devices
- B29B7/34—Mixing; Kneading continuous, with mechanical mixing or kneading devices with movable mixing or kneading devices
- B29B7/38—Mixing; Kneading continuous, with mechanical mixing or kneading devices with movable mixing or kneading devices rotary
- B29B7/46—Mixing; Kneading continuous, with mechanical mixing or kneading devices with movable mixing or kneading devices rotary with more than one shaft
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B29—WORKING OF PLASTICS; WORKING OF SUBSTANCES IN A PLASTIC STATE IN GENERAL
- B29B—PREPARATION OR PRETREATMENT OF THE MATERIAL TO BE SHAPED; MAKING GRANULES OR PREFORMS; RECOVERY OF PLASTICS OR OTHER CONSTITUENTS OF WASTE MATERIAL CONTAINING PLASTICS
- B29B9/00—Making granules
- B29B9/02—Making granules by dividing preformed material
- B29B9/06—Making granules by dividing preformed material in the form of filamentary material, e.g. combined with extrusion
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B29—WORKING OF PLASTICS; WORKING OF SUBSTANCES IN A PLASTIC STATE IN GENERAL
- B29C—SHAPING OR JOINING OF PLASTICS; SHAPING OF MATERIAL IN A PLASTIC STATE, NOT OTHERWISE PROVIDED FOR; AFTER-TREATMENT OF THE SHAPED PRODUCTS, e.g. REPAIRING
- B29C2948/00—Indexing scheme relating to extrusion moulding
- B29C2948/92—Measuring, controlling or regulating
- B29C2948/92504—Controlled parameter
- B29C2948/92704—Temperature
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- B—PERFORMING OPERATIONS; TRANSPORTING
- B29—WORKING OF PLASTICS; WORKING OF SUBSTANCES IN A PLASTIC STATE IN GENERAL
- B29C—SHAPING OR JOINING OF PLASTICS; SHAPING OF MATERIAL IN A PLASTIC STATE, NOT OTHERWISE PROVIDED FOR; AFTER-TREATMENT OF THE SHAPED PRODUCTS, e.g. REPAIRING
- B29C2948/00—Indexing scheme relating to extrusion moulding
- B29C2948/92—Measuring, controlling or regulating
- B29C2948/92819—Location or phase of control
- B29C2948/92857—Extrusion unit
- B29C2948/92876—Feeding, melting, plasticising or pumping zones, e.g. the melt itself
- B29C2948/92895—Barrel or housing
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B29—WORKING OF PLASTICS; WORKING OF SUBSTANCES IN A PLASTIC STATE IN GENERAL
- B29C—SHAPING OR JOINING OF PLASTICS; SHAPING OF MATERIAL IN A PLASTIC STATE, NOT OTHERWISE PROVIDED FOR; AFTER-TREATMENT OF THE SHAPED PRODUCTS, e.g. REPAIRING
- B29C2948/00—Indexing scheme relating to extrusion moulding
- B29C2948/92—Measuring, controlling or regulating
- B29C2948/92819—Location or phase of control
- B29C2948/92857—Extrusion unit
- B29C2948/92904—Die; Nozzle zone
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- Engineering & Computer Science (AREA)
- Mechanical Engineering (AREA)
- Chemical & Material Sciences (AREA)
- Health & Medical Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Medicinal Chemistry (AREA)
- Polymers & Plastics (AREA)
- Organic Chemistry (AREA)
- Compositions Of Macromolecular Compounds (AREA)
- Reinforced Plastic Materials (AREA)
Abstract
The invention discloses a high-glass-fiber reinforced nylon material and a preparing method of the high-glass-fiber reinforced nylon material. The high-glass-fiber reinforced nylon material comprises the following ingredients in percentage by weight: 30 percent to 35 percent of nylon 66, 60 percent to 64 percent of glass fiber, 0.03 percent to 0.05 percent of silane coupling agents, 0.15 percent to 0.2 percent of antioxidants 1010, 0.15 percent to 0.25 percent of antioxidants 1068, 0.6 percent to 1 percent of silicone, 0.35 percent to 0.5 percent of calcium stearate and 3.5 percent to 4.5 percent of talcum powder. The preparing method comprises the following steps that: the PA66, the silane coupling agents, the antioxidants 1010, the antioxidants 1068, the silicone, the calcium stearate and the talcum powder are mixed according to the content mixture ratio; then, the mixture is added into a high-speed stirring pot and is stirred at a high speed for 4 to 6 minutes in room-temperature environment; the stirred raw materials are added into a double-screw extruder; the glass fiber is added from an inlet of the extruder; and after the discharging, pulled strips are rinsed in water for cooling, and grain cutting, drying and packaging are carried out. The high-glass-fiber reinforced nylon material has very high intensity and can be widely applied to automobiles, communication, electronic and electric equipment and mechanical equipment.
Description
Technical field
The present invention relates to a kind of high glass fiber reinforced nylon material, also relate to the preparation method of this high glass fiber reinforced nylon material.
Background technology
Nylon is polyamide resin (PA), and its amide group has polarity, has firmly hydrogen bond in its structure, makes the fusing point of nylon higher, has good mechanical property.Development along with nylon science and technology, the application of nylon in automobile, communication, electronic electric equipment, mechanical means increases gradually, but existing nylon undercapacity, cannot meet the service requirements of engineering equipment, in order to gain in strength, need to add a large amount of glass fibre, but while producing, there will be the not problem of poor effect of glass fibre mix and blend, the nylon material intensity of therefore producing or inadequate, and also work-ing life is short.
Summary of the invention
The deficiency existing for prior art, the object of the present invention is to provide a kind of wear resistance good, nylon material that intensity is high and preparation method thereof.
For achieving the above object, the invention provides following technical scheme: a kind of high glass fiber reinforced nylon material, by weight percentage, its component and content are:
Nylon 66 30%-35%
Glass fibre 60%-64%
Silane coupling agent 0.03%-0.05%
Antioxidant 1010 0.15%-0.2%
Oxidation inhibitor 1068 0.15%-0.25%
Silicone 0.6%-1%
Calcium stearate 0.35%-0.5%
Talcum powder 3.5%-4.5%.
A method of preparing described high glass fiber reinforced nylon material, comprises the steps:
(1) press content proportioning by after PA66, silane coupling agent, antioxidant 1010, oxidation inhibitor 1068, silicone, calcium stearate, talcum powder mixing, add high-speed stirring pot, rotating speed is controlled at 400-500r/min, under room temperature environment, stirs 4-6 minute;
(2) raw material being stirred is added to twin screw extruder, glass fibre is added by forcing machine ingress, temperature in twin screw extruder is respectively: 280 ℃ of district's temperature, 280 ℃ of two district's temperature, 280 ℃ of three district's temperature, 275 ℃ of four district's temperature, 270 ℃ of five district's temperature, 270 ℃ of six district's temperature, 260 ℃ of seven district's temperature, 260 ℃ of eight district's temperature, die head temperature is 280 ℃, vacuum pressure >=0.08pa, after discharging, tie rod is crossed water cooling, pelletizing, dry, packing.
In nylon, nylon 66 has higher fusing point, higher intensity and better wear resistance, therefore select nylon 66, is major ingredient.
Glass fibre has good thermotolerance and higher physical strength, can increase accordingly resistance toheat and the intensity of this nylon.
Silane coupling agent can be erected " molecular bridge " between inorganic substance and the interface of organic substance, and the material of two kinds of character great disparities is linked together, and improves the effect of performance and the increase bonding strength of matrix material.
Antioxidant 1010 is a kind of hindered phenol antioxygen of high molecular, and volatility is very low, and is difficult for migration, and resistance to extraction can improve the antioxygen property of this nylon, can effectively extend the work-ing life of goods; Antioxidant 1010 is also a kind of efficient processing stabilizers simultaneously, can improve the discoloration-resistant of polymer materials under high temperature process condition.
Oxidation inhibitor 1068 is composite products of antioxidant 1010 and irgasfos 168, and compound oxidation inhibitor 1068 has lower cost, better than the antioxidant effect of independent use irgasfos 168 or antioxidant 1010.
Silicone can improve the mobility of this nylon processing, reduces equipment attrition.
Calcium stearate can increase the workability of this nylon when extrusion moulding and compression moulding, makes nylon molding more laborsaving, greatly reduces production difficulty, has improved production efficiency.
Good physics, the chemical property such as talcum powder has that oilness, resistivity against fire, fusing point are high, good luster, adsorptive power are strong, because the crystal structure of talcum is stratiform, so have, easily split into the trend of scale and special slip, can effectively improve lubricity, the flame retardant properties of this nylon.
The invention has the beneficial effects as follows: content of glass fiber of the present invention is higher, make this nylon product there is high intensity, in nylon 66, add silicone and calcium stearate, make it when producing, improve mobility and the workability of mixture, what make that it mixes with glass fibre is more abundant, add silane coupling agent can improve the bonding strength of this nylon material simultaneously, by talcum powder, increase lubricity and the flame retardant properties of this nylon material simultaneously, by the synergy of antioxidant 1010 and oxidation inhibitor 1068, improve the antioxygen property of this nylon material, can be widely used in automobile, communication, electronic electric equipment, in mechanical means, not only meet the service requirements of engineering plastics, and there is higher work-ing life.
Embodiment
Below with reference to specific embodiment, the invention will be further described, but protection scope of the present invention is not limited to this.
A high glass fiber reinforced nylon material, by weight percentage, its component and content are:
Nylon 66 30%-35%
Glass fibre 60%-64%
Silane coupling agent 0.03%-0.05%
Antioxidant 1010 0.15%-0.2%
Oxidation inhibitor 1068 0.15%-0.25%
Silicone 0.6%-1%
Calcium stearate 0.35%-0.5%
Talcum powder 3.5%-4.5%.
Group and each component concentration containing for the high glass fiber reinforced nylon material of embodiment of the present invention 1-3 as shown in table 1.
The group that the high glass fiber reinforced nylon material of table 1 embodiment 1-3 contains and each component concentration
Matrix material contains component and each component concentration | Embodiment 1 | Embodiment 2 | Embodiment 3 |
Nylon 66 | 30% | 32% | 35% |
Glass fibre | 64% | 63% | 60% |
Silane coupling agent | 0.04% | 0.03% | 0.05% |
Antioxidant 1010 | 0.2% | 0.17% | 0.15% |
Oxidation inhibitor 1068 | 0.25% | 0.2% | 0.15% |
Silicone | 0.6% | 0.1% | 0.8% |
Calcium stearate | 0.41% | 0.5% | 0.35% |
Talcum powder | 4.5% | 4% | 3.5% |
The preparation method of this high glass fiber reinforced nylon material is as follows:
(1) press content proportioning by after PA66, silane coupling agent, antioxidant 1010, oxidation inhibitor 1068, silicone, calcium stearate, talcum powder mixing, add high-speed stirring pot, rotating speed is controlled at 400-500r/min, stirs 5 minutes under room temperature environment;
(2) raw material being stirred is added to twin screw extruder, glass fibre is added by forcing machine ingress, temperature in twin screw extruder is respectively: 280 ℃ of district's temperature, 280 ℃ of two district's temperature, 280 ℃ of three district's temperature, 275 ℃ of four district's temperature, 270 ℃ of five district's temperature, 270 ℃ of six district's temperature, 260 ℃ of seven district's temperature, 260 ℃ of eight district's temperature, die head temperature is 280 ℃, vacuum pressure >=0.08pa, after discharging, tie rod is crossed water cooling, pelletizing, dry, packing.
After doing detection according to the nylon material of embodiment 3 preparations, it is reported as follows:
examining report
Test item | Testing standard | Unit | Measured data |
Glass | GB/ 9345.1-2008 | % | 60 |
Tensile strength | GB/T 1040.2-2006 | MPa | 230 |
Elongation at break | GB/T 1040.2-2006 | % | 2.5 |
Flexural strength | GB/T 9341-2008 | MPa | 340 |
Modulus in flexure | GB/T 9341-2008 | MPa | 15600 |
Simple beam impact strength (breach) | GB/T 1043.1-2008 | kJ/m 2 | 23 |
Cantilever beam impact strength (breach) | GB/T 1843.1-2008 | kJ/m 2 | 13 |
Heat-drawn wire | GB/T 1634.2-2004 | ℃ | 255 |
Claims (2)
1. a high glass fiber reinforced nylon material, is characterized in that, by weight percentage, its component and content are:
Nylon 66 30%-35%
Glass fibre 60%-64%
Silane coupling agent 0.03%-0.05%
Antioxidant 1010 0.15%-0.2%
Oxidation inhibitor 1068 0.15%-0.25%
Silicone 0.6%-1%
Calcium stearate 0.35%-0.5%
Talcum powder 3.5%-4.5%.
2. a method of preparing high glass fiber reinforced nylon material claimed in claim 1, is characterized in that, comprises the steps:
(1) press content proportioning by after PA66, silane coupling agent, antioxidant 1010, oxidation inhibitor 1068, silicone, calcium stearate, talcum powder mixing, add high-speed stirring pot, rotating speed is controlled at 400-500r/min, under room temperature environment, stirs 4-6 minute;
(2) raw material being stirred is added to twin screw extruder, glass fibre is added by forcing machine ingress, temperature in twin screw extruder is respectively: 280 ℃ of district's temperature, 280 ℃ of two district's temperature, 280 ℃ of three district's temperature, 275 ℃ of four district's temperature, 270 ℃ of five district's temperature, 270 ℃ of six district's temperature, 260 ℃ of seven district's temperature, 260 ℃ of eight district's temperature, die head temperature is 280 ℃, vacuum pressure >=0.08pa, after discharging, tie rod is crossed water cooling, pelletizing, dry, packing.
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Cited By (5)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN104859928A (en) * | 2015-04-17 | 2015-08-26 | 柳州蔚园塑料彩印包装有限责任公司 | Manufacturing method for express plastic packaging bags |
CN105131592A (en) * | 2015-08-31 | 2015-12-09 | 宁波海雨新材料科技有限公司 | High-content glass fiber reinforced polyamide 66 composite material and preparing method |
CN107949602A (en) * | 2015-09-17 | 2018-04-20 | 陶氏环球技术有限责任公司 | With the polymer coating composition for reducing ignition sensitivity |
CN109438979A (en) * | 2018-11-22 | 2019-03-08 | 浙江华谊胜德材料科技有限公司 | A kind of high smooth engineering plastic alloy and preparation method thereof |
CN114316585A (en) * | 2022-01-08 | 2022-04-12 | 浙江卡尼尔聚合新材料有限公司 | High-strength nylon 66 composite material and processing technology thereof |
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JPH11293106A (en) * | 1998-04-09 | 1999-10-26 | Mitsubishi Eng Plast Corp | Reinforced polyamide resin composition |
CN101215417A (en) * | 2007-12-28 | 2008-07-09 | 深圳市科聚新材料有限公司 | Hexamethylene diamine adipate fibre-adding modified engineering plastics and preparation method thereof |
CN102061088A (en) * | 2010-12-10 | 2011-05-18 | 南京聚隆科技股份有限公司 | Nylon engineering plastics for high-speed transit railway track and manufacture method thereof |
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2014
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Patent Citations (3)
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JPH11293106A (en) * | 1998-04-09 | 1999-10-26 | Mitsubishi Eng Plast Corp | Reinforced polyamide resin composition |
CN101215417A (en) * | 2007-12-28 | 2008-07-09 | 深圳市科聚新材料有限公司 | Hexamethylene diamine adipate fibre-adding modified engineering plastics and preparation method thereof |
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Cited By (8)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN104859928A (en) * | 2015-04-17 | 2015-08-26 | 柳州蔚园塑料彩印包装有限责任公司 | Manufacturing method for express plastic packaging bags |
CN105131592A (en) * | 2015-08-31 | 2015-12-09 | 宁波海雨新材料科技有限公司 | High-content glass fiber reinforced polyamide 66 composite material and preparing method |
CN105131592B (en) * | 2015-08-31 | 2018-07-06 | 宁波海雨新材料科技有限公司 | A kind of high-content glass fiber enhanced nylon 66 composite material and preparation method |
CN107949602A (en) * | 2015-09-17 | 2018-04-20 | 陶氏环球技术有限责任公司 | With the polymer coating composition for reducing ignition sensitivity |
CN107949602B (en) * | 2015-09-17 | 2020-11-27 | 陶氏环球技术有限责任公司 | Polymer coating compositions having reduced ignition sensitivity |
CN109438979A (en) * | 2018-11-22 | 2019-03-08 | 浙江华谊胜德材料科技有限公司 | A kind of high smooth engineering plastic alloy and preparation method thereof |
CN114316585A (en) * | 2022-01-08 | 2022-04-12 | 浙江卡尼尔聚合新材料有限公司 | High-strength nylon 66 composite material and processing technology thereof |
CN114316585B (en) * | 2022-01-08 | 2024-01-02 | 浙江卡尼尔聚合新材料有限公司 | High-strength nylon 66 composite material and processing technology thereof |
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